Medical affairs jobs in Southall

Extensive experience in Regulatory Affairs with experience acting as therapeutic area European Regulatory Affairs lead, defining and implement regulatory strategies and executional plans. Define and advise the GRT on regional considerations in developing creative regulatory strategy, lead develop...

Collaborate with the Senior Manager of Medical Engagement and the Head of Medical Affairs to develop and implement the Medical Affairs strategic and operational plan, aligning with business goals and stakeholder needs. The successful candidate will develop, communicate, and implement the Medical ...

The Medical Affairs Lead is responsible for providing Medical Information, Training and Support across all areas of the companies product portfolio, you will also be tasked with developing a Medical Affairs strategy and department that meets the needs of a growing business. Experience of working ...

Associate Director, Medical Affairs. If you're a strategic innovator within Medical Affairs, this is an opportunity for you. ...

You will have vendor support for medical writing through Global agencies and they will have internal support from the medical team. Experience of working in medical affairs in the pharmaceutical industry. Possible experienced in vendor medical communication environment. Medical writing for scient...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading global drug development organization. We are seeking a motivated individual with substantial experience in Medical Device Regulation, particularly in the areas of combination pr...

Regulatory Affairs Associate Manager - Cosmetics. Planet Pharma are partnered with a niche mid-sized CRO assisting them with the search for an Associate Manager, Regulatory Affairs to work on an initial 6+ month project with a focus on Cosmetic products. The Associate Manager will ensure products...

Join a dynamic and ambitious truly independent agency as a Senior Medical Writer and immerse yourself in diverse, exciting meded, med affairs and omnichannel projects. ...

Haybury is thrilled to announce a new partnership on a fantastic opportunity for a Senior Medical Writer. Proven experience in a Medical Writer role. Participate and develop medical education programs. ...

Associate Director Regulatory Affairs. Works with the Lead, Regulatory Affairs, and the Development Team, and with moderate/minimal supervision, with select project teams within subsidiary organizations to develop and oversee program-specific regulatory, clinical, and development strategies. Resp...

Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone regulatory project, with guidance from senior staff as appropriate. May write new regulatory SOPs and regulatory intelligence databanks, and/or propose r...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Main...

The role will encompass a large percentage of medical affairs work, as well as some promotional (and no publications!) The ideal candidate will have a blend of creative, visual experience, as well as the knowledge and confidence to work across high science accounts/projects. ...

Remote Senior Regulatory Medical Writer working through an FSP model for a Global Oncology focused Pharmaceutical Company. The Principal Medical Writer I is responsible for developing clinical documents for submissions to regulatory authorities globally. Oversees the medical writing activities of...

Senior Director of Medical Strategy (Cardiovascular). A global CRO is seeking a Senior Director to join their Cardiovascular unit. This organisation is looking to welcome the new Senior Director onboard as soon as possible. ...

Senior Regulatory Affairs Specialist who will be responsible for planning, creating, and implementing solutions for regulatory registration and release of products for distribution into specific geographies. Senior Regulatory Affairs Specialist – Medical Devices & IVD’s. Minimum of 4 to 5 years p...

Publications, medical communications, medical education, congress activities. If you’re an experienced writer, seeking to join a team of strong writers and have mentoring responsibilities, this could be a great fit! We’re looking for someone who has:. At least 3 years of experience working as a w...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to suppo...

You're an established Senior Medical Writer, with either Medical Affairs or Publications experience, looking for the next challenge, or an experienced Medical Writer aiming to move up. Senior Medical Writers define new directions with CMC Affinity. IPG Health Medical Communications is home to the...

VP, Medical Director, CMC Affinity - UK. We are CMC Affinity, and we are hiring for an VP, Medical Director to join our global team, based in the UK. IPG Health Medical Communications is home to the world’s most celebrated and awarded med comms agencies, united by a healthy obsession with creatin...

The successful Medical Science Liaison will be working with the medical team to communicate evidence based scientific, technical and development matters with customers and stakeholders. Acting as the field scientific / medical expert, delivering medical education, updates and gathering insights a...

CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Regulatory Affairs Associate Role:. Experience in a Regulatory Affairs role in CMC, including preparation of submissions to Agencies and fami...

Experience of working in medical affairs in the pharmaceutical industry * Therapeutic area experience of neurological disorders would be a plus * Possible experienced in vendor medical communication ...